Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20456674-20457142 | Common:2; Rare:182; Clinvar:2 | ||||
chr14:21194653-21194688 | Rare:6 | ||||
chr14:21199647-21199717 | Rare:15 | ||||
chr14:21200270-21200346 | Rare:11 | ||||
chr14:21202753-21202906 | Common:1; Rare:34 | ||||
chr14:21206075-21206339 | Common:4; Rare:82 | ||||
chr14:21220854-21220971 | Rare:28 | ||||
chr14:21247325-21247556 | Common:1; Rare:53 | ||||
chr14:21249238-21249281 | Rare:10 | ||||
chr14:21252110-21252295 | Rare:31 | ||||
chr14:21257683-21257776 | Rare:22 | ||||
chr14:21259528-21259731 | Rare:37 | ||||
chr14:21267295-21267549 | Common:1; Rare:60 | ||||
chr14:21267555-21267823 | Rare:59 | ||||
chr14:21360930-21361161 | Common:1; Rare:58 |